symbol withdrawn PDB2

Preferred Label : symbol withdrawn PDB2;

Obsolete resource : true;

Approved symbol HGNC : PDB2;

Alias symbols HGNC : FEO;

Chromosome HGNC : 18q;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:8758;

Automatic exact mappings (from CISMeF team)
- Familial expansile osteolysis [OMIM Phenotype]
- Paget disease of bone 2, early-onset [OMIM Phenotype]
Replaced by
- TNF receptor superfamily member 11a [HGNC gene]

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